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Combination of Anti-CD40 and Anti-CD40L Antibodies as Co-Stimulation Blockade in Preclinical Cardiac Xenotransplantation.
Bender, Martin; Abicht, Jan-Michael; Reichart, Bruno; Neumann, Elisabeth; Radan, Julia; Mokelke, Maren; Buttgereit, Ines; Leuschen, Maria; Wall, Felicia; Michel, Sebastian; Ellgass, Reinhard; Steen, Stig; Paskevicius, Audrius; Lange, Andreas; Kessler, Barbara; Kemter, Elisabeth; Klymiuk, Nikolai; Denner, Joachim; Godehardt, Antonia W; Tönjes, Ralf R; Burgmann, Jonathan M; Figueiredo, Constança; Milusev, Anastasia; Zollet, Valentina; Salimi-Afjani, Neda; Despont, Alain; Rieben, Robert; Ledderose, Stephan; Walz, Christoph; Hagl, Christian; Ayares, David; Wolf, Eckhard; Schmoeckel, Michael; Brenner, Paolo; Binder, Uli; Gebauer, Michaela; Skerra, Arne; Längin, Matthias.
Afiliação
  • Bender M; Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany.
  • Abicht JM; Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany.
  • Reichart B; Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany.
  • Neumann E; Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany.
  • Radan J; Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany.
  • Mokelke M; Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany.
  • Buttgereit I; Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany.
  • Leuschen M; Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany.
  • Wall F; Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany.
  • Michel S; Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany.
  • Ellgass R; Munich Heart Alliance, German Center for Cardiovascular Research (DZHK), 81377 Munich, Germany.
  • Steen S; Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany.
  • Paskevicius A; Department of Cardiothoracic Surgery, Lund University and Skåne University Hospital, 22242 Lund, Sweden.
  • Lange A; Department of Cardiothoracic Surgery, Lund University and Skåne University Hospital, 22242 Lund, Sweden.
  • Kessler B; Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany.
  • Kemter E; Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany.
  • Klymiuk N; Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany.
  • Denner J; Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany.
  • Godehardt AW; Institute of Virology, Free University Berlin, 14163 Berlin, Germany.
  • Tönjes RR; Division of Haematology, Cell and Gene Therapy, Paul-Ehrlich-Institut, 63225 Langen, Germany.
  • Burgmann JM; Division of Haematology, Cell and Gene Therapy, Paul-Ehrlich-Institut, 63225 Langen, Germany.
  • Figueiredo C; Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, 30625 Hannover, Germany.
  • Milusev A; Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, 30625 Hannover, Germany.
  • Zollet V; Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland.
  • Salimi-Afjani N; Graduate School for Cellular and Biomedical Sciences (GCB), University of Bern, 3008 Bern, Switzerland.
  • Despont A; Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland.
  • Rieben R; Graduate School for Cellular and Biomedical Sciences (GCB), University of Bern, 3008 Bern, Switzerland.
  • Ledderose S; Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland.
  • Walz C; Graduate School for Cellular and Biomedical Sciences (GCB), University of Bern, 3008 Bern, Switzerland.
  • Hagl C; Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland.
  • Ayares D; Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland.
  • Wolf E; Institute of Pathology, Faculty of Medicine, LMU Munich, 81377 Munich, Germany.
  • Schmoeckel M; Institute of Pathology, Faculty of Medicine, LMU Munich, 81377 Munich, Germany.
  • Brenner P; Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany.
  • Binder U; Munich Heart Alliance, German Center for Cardiovascular Research (DZHK), 81377 Munich, Germany.
  • Gebauer M; Revivicor, Blacksburg, VA 24060, USA.
  • Skerra A; Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany.
  • Längin M; Center for Innovative Medical Models (CiMM), LMU Munich, 81377 Munich, Germany.
Biomedicines ; 12(8)2024 Aug 22.
Article em En | MEDLINE | ID: mdl-39200391
ABSTRACT
The blockade of the CD40/CD40L immune checkpoint is considered essential for cardiac xenotransplantation. However, it is still unclear which single antibody directed against CD40 or CD40L (CD154), or which combination of antibodies, is better at preventing organ rejection. For example, the high doses of antibody administered in previous experiments might not be feasible for the treatment of humans, while thrombotic side effects were described for first-generation anti-CD40L antibodies. To address these issues, we conducted six orthotopic pig-to-baboon cardiac xenotransplantation experiments, combining a chimeric anti-CD40 antibody with an investigational long-acting PASylated anti-CD40L Fab fragment. The combination therapy effectively resulted in animal survival with a rate comparable to a previous study that utilized anti-CD40 monotherapy. Importantly, no incidence of thromboembolic events associated with the administration of the anti-CD40L PAS-Fab was observed. Two experiments failed early because of technical reasons, two were terminated deliberately after 90 days with the baboons in excellent condition and two were extended to 120 and 170 days, respectively. Unexpectedly, and despite the absence of any clinical signs, histopathology revealed fungal infections in all four recipients. This study provides, for the first time, insights into a combination therapy with anti-CD40/anti-CD40L antibodies to block this immune checkpoint.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article